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Article

An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.

Human molecular genetics - 1 Feb 1997

Wevrick R, Francke U

Abstract excerpt

The Prader-Willi syndrome (PWS) is caused by genomic alterations that inactivate imprinted, paternally expressed genes in human chromosome region 15q11-q13. IPW, a paternally expressed gene cloned from this region, is not expressed in individuals with PWS, and is thus a candidate for involvement in this disorder. The IPW transcript does not appear to encode a polypeptide, suggesting that it functions at the level...

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Identifiers

PMID: 9063754
DOI: 10.1093/hmg/6.2.325

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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